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Results 1 - 1 of 1 for "17q21.31" microdeletion syndrome
  1. KANSL1 gene 
    ... JA, Eichler EE. Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing. Am J Hum Genet. ... in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. Nat Genet. 2012 Apr 29;44(6):639- ...
    https://medlineplus.gov/genetics/gene/kansl1 - Genetics